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1
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22144446800
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For the Pd-assisted allylation of oximes, see:
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For the Pd-assisted allylation of oximes, see:. Miyabe H., Yoshida K., Reddy V.K., Matsumura A., and Takemoto Y. J. Org. Chem. 70 (2005) 5630-5635
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Miyabe, H.1
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Matsumura, A.4
Takemoto, Y.5
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2
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5644243295
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Miyabe H., Matsumura A., Yoshida K., Yamauchi M., and Takemoto Y. Synlett (2004) 2123-2126
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Miyabe, H.1
Matsumura, A.2
Yoshida, K.3
Yamauchi, M.4
Takemoto, Y.5
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3
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0001568867
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For deprotection of allyl group, see:
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For deprotection of allyl group, see:. Yamada T., Goto K., Mitsuda Y., and Tsuji J. Tetrahedron Lett. 28 (1987) 4557-4560
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Yamada, T.1
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Ohno H., Aso A., Kadoh Y., Fujii N., and Tanaka T. Angew. Chem., Int. Ed. 46 (2007) 6325-6328
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Ohno, H.1
Aso, A.2
Kadoh, Y.3
Fujii, N.4
Tanaka, T.5
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7
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0037221784
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For the Pd-catalyzed amino-Heck reactions of oxime derivatives, see:
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For the Pd-catalyzed amino-Heck reactions of oxime derivatives, see:. Narasaka K. Pure Appl. Chem. 75 (2003) 19-28
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(2003)
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Narasaka, K.1
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and further references cited therein
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Kitamura M., and Narasaka K. Chem. Rec. 2 (2002) 268-277 and further references cited therein
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Kitamura, M.1
Narasaka, K.2
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14
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48849116985
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For the miscellaneous reactions of oximes, see:
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For the miscellaneous reactions of oximes, see:. Jiang D., Peng J., and Chen Y. Org. Lett. 10 (2008) 1695-1698
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(2008)
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Jiang, D.1
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1042264358
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2], see:
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2], see:. Makarycheva-Mikhailova A.V., Bokach N.A., Haukka M., and Kukushkin V.Y. Inorg. Chim. Acta 356 (2003) 382-386
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Makarycheva-Mikhailova, A.V.1
Bokach, N.A.2
Haukka, M.3
Kukushkin, V.Y.4
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20
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0000555841
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For examples, on the synthesis of nitriles from oximes, see:
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For examples, on the synthesis of nitriles from oximes, see:. Yang S.H., and Chang S. Org. Lett. 3 (2001) 4209-4211
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(2001)
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Yang, S.H.1
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Yamaguchi K., Fujiwara H., Ogasawara Y., Kotani M., and Mizuno N. Angew. Chem., Int. Ed. 46 (2007) 3922-3925
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Yamaguchi, K.1
Fujiwara, H.2
Ogasawara, Y.3
Kotani, M.4
Mizuno, N.5
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30
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50949088404
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For our recent contribution on Pd-mediated decarboxylative protonation and allylation, see: and further references on Pd-mediated protonation and allylation reactions were cited therein
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For our recent contribution on Pd-mediated decarboxylative protonation and allylation, see:. Gowrisankar S., Kim K.H., Kim S.H., and Kim J.N. Tetrahedron Lett. 49 (2008) 6241-6244 and further references on Pd-mediated protonation and allylation reactions were cited therein
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Gowrisankar, S.1
Kim, K.H.2
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Kim, J.N.4
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31
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36849051972
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For the Pd-mediated decarboxylative allylation and related reactions involving nitro arene or pyridine moiety, see:
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For the Pd-mediated decarboxylative allylation and related reactions involving nitro arene or pyridine moiety, see:. Waetzig S.R., and Tunge J.A. J. Am. Chem. Soc. 129 (2007) 14860-14861
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Waetzig, S.R.1
Tunge, J.A.2
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33
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25844476804
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3; however, detailed mechanism and scope of this novel finding needs further study. For the use of tetraarylphosphonium halides as arylating reagents in Pd-catalyzed Heck and cross-coupling reactions, see:
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3; however, detailed mechanism and scope of this novel finding needs further study. For the use of tetraarylphosphonium halides as arylating reagents in Pd-catalyzed Heck and cross-coupling reactions, see:. Hwang L.K., Na Y., Lee J., Do Y., and Chang S. Angew. Chem., Int. Ed. 44 (2005) 6166-6169
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Hwang, L.K.1
Na, Y.2
Lee, J.3
Do, Y.4
Chang, S.5
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34
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60649117575
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note
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3CN (1.5 mL) was heated to reflux for 3 h. The reaction mixture was filtered through a Celite pad, washed with EtOAc, and the solvent was removed. After column chromatographic purification process (hexanes/EtOAc, 8:1), analytically pure p-nitrobenzonitrile was isolated, 67 mg (90%) as a white solid.
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35
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0001601002
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For the reactions involving L-Pd-OH intermediate, see:
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For the reactions involving L-Pd-OH intermediate, see:. Hosokawa T., Sugafuji T., Yamanaka T., and Murahashi S.-I. J. Organomet. Chem. 470 (1994) 253-255
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(1994)
J. Organomet. Chem.
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Hosokawa, T.1
Sugafuji, T.2
Yamanaka, T.3
Murahashi, S.-I.4
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38
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0032839744
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For the possibility of anti-β-hydride elimination, see: and further references cited therein
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For the possibility of anti-β-hydride elimination, see:. Schwarz I., and Braun M. Chem. Eur. J. 5 (1999) 2300-2305 and further references cited therein
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Chem. Eur. J.
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Schwarz, I.1
Braun, M.2
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39
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60649086192
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note
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3, reflux, 36 h) showed no reaction.
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40
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60649086959
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note
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3, 3 h).
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